EP0725797B1 - Inhibiteurs bivalents de thrombine - Google Patents

Inhibiteurs bivalents de thrombine Download PDF

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EP0725797B1
EP0725797B1 EP94930133A EP94930133A EP0725797B1 EP 0725797 B1 EP0725797 B1 EP 0725797B1 EP 94930133 A EP94930133 A EP 94930133A EP 94930133 A EP94930133 A EP 94930133A EP 0725797 B1 EP0725797 B1 EP 0725797B1
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glu
acid
pro
arg
tyr
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EP0725797A1 (fr
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Yasuo Konishi
Zbigniew Szewczuk
Yuko Tsuda
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National Research Council of Canada
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National Research Council of Canada
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/81—Protease inhibitors
    • C07K14/815—Protease inhibitors from leeches, e.g. hirudin, eglin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • thrombin plays a central role in the coagulation cascade of higher animals.
  • the primary function of thrombin is to activate fibrinogen to fibrin and generate an insoluble fibrin clot. It also serves regulatory functions in coagulopathy by activating several participating cofactors and proteases such as factor V, factor VIII, factor XIII and protein C.
  • thrombin promotes coagulopathy, activates platelets and causes secretion of granular substances that exacerbate the condition.
  • Thrombin's interaction with endothelial cells, smooth muscle cells, fibroblasts, and monocytes/macrophages contribute further to the inflammatory process in thrombotic events.
  • An acute blockage of a coronary artery by a thrombus causes a myocardial infarction. In its early stages, the condition may be alleviated with thrombolytic therapy.
  • typical thrombolysis with tissue plasminogen activator, urokinase or streptokinase is problematic.
  • Acute thrombotic reocclusion often occurs after initial successful thrombolysis using these agents.
  • thrombus-bound thrombin may contribute to this problem. Potent and specific agents that neutralize thrombus-bound thrombin would be desirable.
  • Thrombin is a member of the trypsin family of serine proteases.
  • the catalytic triad Asp 102, His 57 and Ser 195
  • a feature common to the active site of all serine proteases, asp 189 in the primary substrate binding site (S1) of the trypsin family plays an important role in the recognition and binding of substrates and inhibitors.
  • heparin A natural anticoagulant, heparin inhibits thrombin through a mechanism requiring a heparin-antithrombin III compounds. Heparin is known to be poorly accessible to thrombus-bound thrombin. Furthermore, heparin often causes bleeding when used therapeutically and is unable to prevent the occlusive complications in atherosclerotic vascular diseases or reocclusion following successful thrombolysis.
  • Hirudin is produced by the salivary glands of the European medicinal leech Hirudo medicinalis and is a small protein of 65 amino acid residues. It has several potential advantages over other antithrombotics. It is the most potent and specific thrombin inhibitor known having a K i value of 2.2 x 10 -14 M. Hirudin blocks the active site (AS) and the fibrinogen recognition exosite (FRE) of thrombin simultaneously. Hirudin also inhibits thrombus-bound thrombin as well as circulating thrombin and it has a long half-life of 30-60 minutes when given intravenously or subcutaneously, depending on the species. Hirudin has very weak antigenicity, and it has no reported acute side effects following intravenous or subcutaneous administration.
  • Synthetic thrombin inhibitors based on the hirudin sequence offer an advantage over native hirudin. They mimic the distinctive mechanism of hirudin and are more readily available through chemical synthesis.
  • the crystal structure of the human ⁇ -thrombin/hirudin complex reveals that hirudin interacts with the enzyme through an active site inhibitor domain (hirudin 1-48 ), a FRE inhibitor segment (hirudin 55-65 ), and a linker segment (hirudin 49-54 ) which connects these binding components.
  • the bulky active site inhibitor segment, hirudin 1-48 is sufficiently large and serves to obstruct the enzyme surface. This action has been shown to be simulated when hirudin 1-48 is replaced by a small active site inhibitor segment, D-Phe-Pro-Arg-Pro, with some loss in inhibitory potency (Maraganore, J.M., Bourdon, P., Jablonsky, J., Ramachandran, K.L., & Fenton, J.W. 11 (1990) Biochemistry 29, 7095-7101; DiMaio, J., Gibbs, B., Munn, D., Lefebvre, J.
  • D-Phe-Pro-Arg-Pro or its analog in the design of active site inhibitors.
  • the crystal structure of D-Phe-Pro-Arg chloromethylketone (PPACK)-thrombin suggested that the D-Phe-Pro-Arg-Pro in bivalent inhibitors bind to the thrombin active site in a substrate binding mode, wherein Arg-X is the scissile peptide bond.
  • the active site inhibitor segment, D-Phe-Pro-Arg-Pro, of the bivalent inhibitors is known to be hydrolyzed slowly by thrombin (DiMaio, J., Gibbs, B., Munn, D., Lefebvre, J., Ni, F. and Konishi, Y. (1990) J.
  • Hirulog-8TM is a bivalent thrombin inhibitor composed of the substrate type inhibitor (D-Phe)-Pro-Arg-Pro, and the native sequence of the hirudin exosite segment 52-65 both linked through a suitable linker (Maraganore et al. US Patent 5,196,404). Since the structure of those thrombin inhibitor is very similar to the structure of hirudin, the interactions of the substrate type active site inhibitor with thrombin are the same as the interactions between the active site of hirudin and thrombin. In addition, it has been shown that the portion (D-Phe)-Pro-Arg-CO can be used in a bivalent thrombin inhibitor (DiMaio et al. International publication WO 91/19734).
  • the use of the acetyl function at the scissile position gives more resistance to enzyme degradation without affecting the inhibitory activity.
  • the scissile position in a substrate is a position that is recognised by the enzyme and where the hydrolysis takes place. It is therefore advantageous to eliminate or to modify the scissile position in order to give to more resistance to enzyme degradation. Since the structure of the two classes of bivalent thrombin inhibitors mentioned above are similar to the structure of hirudin, their synthesis is difficult, cumbersome, uses dangerous chemicals and affords low yields of the desired compounds. There is therefore a need for other thrombin inhibitors that would combine high inhibiting activity, enzyme resistance and affordable synthesis.
  • nonsubstrate type inhibitors could be designed to block the active site of thrombin without being cleaved.
  • examples of these may be derived from arginine and benzamidine to give, for example, (2R,4R)-4-methyl-1-[N ⁇ -(3-methyl-1,2,3,4-tetrahydro-8-quinolinesulphonyl)-L-arginyl]-2-piperidine carboxylic acid (MD-805), N ⁇ -(4-toluene-sulphonyl)-D,L-amidinophenylalanyl-piperidine (TAPAP), and N ⁇ -(2-naphthyl-sulphonyl-glycyl)-D-L, p -amidinophenylalanylpiperidine (NAPAP).
  • active-site directed synthetic inhibitors have a short half-life of less than several minutes in the circulation. This activity is not of sufficient duration to be effective against the continuous production of thrombin by the patient or against the effect of liberated thrombus bound-thrombin.
  • the characteristic sequence of these compounds starting from the N-terminus is an aromatic group, arginyl or benzamidyl, and piperidide or its analogs. In contrast to hirudin-based sequences, these moieties would be expected to occupy the S3, S1 and S2 subsites of the thrombin active site, respectively.
  • incorporation of a non-substrate type active site inhibitor into the bivalent inhibitor may have advantages over the substrate like counterparts.
  • a linker attached to the P2 residue piperidide or its analogs could eliminate a labile peptide bond that normally spans the scissile position.
  • the potency of the bivalent inhibitor might be improved because of the higher affinity of the non-substrate type active site-directed segment.
  • a shortened thrombin inhibitor of the hirudin type It would be desirable to develop a shortened thrombin inhibitor of the hirudin type. Such a shortened sequence would be easier to synthesize and cheaper to produce. It would have a drastically shortened linear sequence and would be less subject to enzymatic degradation in a mammal.
  • WO 93/22344 discloses thrombin inhibiting compounds of the type AS-Z-ES, wherein AS is an active site portion, Z is a linker and ES is an exosite portion.
  • AS portion comprises a para-substituted piperidine analogue.
  • the invention seeks to provide improved bivalent inhibitors having increased potency and proteolytic stability comprising non-substrate type active site inhibitor segment.
  • the amount of product, 7-amino-4-methylcoumarin is plotted at a substrate concentration of (A) 40 ⁇ M or (B) 4 ⁇ M and as a function of various concentrations of inhibitors as a function of time.
  • Table I shows K i and IC 50 values for several thrombin active site directed inhibitors. Their inhibition was analyzed using the method in Segel 1975.
  • Table II shows the K i activity values for bivalent inhibitors with various active site inhibitor segments.
  • the exosite segment in all of the examples corresponds to the amino acid sequence of the exosite on natural hirudin.
  • Table III shows the effect of variations within the linker segment Z (the spacer function) on the K i and IC 50 values of the resulting thrombin inhibitors.
  • Table IV shows the effect of the variations within the fibrinogen recognition exosite inhibitor segment, G-X 2 -G 1 -Q-X 3 -R 2 , on the K i values of the resulting thrombin inhibitors.
  • Table V shows the effect of the variations within the active site segment, the linker segment Z and the fibrinogen recognition exosite inhibitor segment, G-X 2 -G 1 -Q-X 3 -R 2 , on the K i values and IC 50 of the resulting thrombin inhibitors.
  • Table VI shows the effect of the variations within the active site segment, the linker segment Z and the fibrinogen recognition exosite inhibitor segment, G-X 2 -G 1 -Q-X 3 -R 2 in the carotid injury-induced thrombosis assay.
  • the combination dansyl-arginyl-pipecolic acid and its derivatives have a very strong hirudin-like activity when combined with the natural hirudin exosite oligopeptide sequence - or an analogue thereof - via a suitable linker sequence.
  • the surprising properties of the compounds of this invention reside in the fact that unlike other known bivalent inhibitor, the active site portion of the compound of this invention is a non-substrate-type inhibitor which binds to thrombin in a different S3,S1,S2 pattern. It was therefore surprising that the non-substrate-type active site inhibitor was able to conserve its inhibiting properties in a bivalent form.
  • the length of the linker of the compounds of the present invention had to be modified because of the different binding pattern of the active site inhibitor.
  • the compounds of the invention are at least 1000 times more active than the dansyl-arginyl-pipecolic acid sequence alone.
  • the dansylated arginyl pipecolamide compounds acquire dramatically enhanced thrombin specificity when compounded with an exosite recognizing sequence via a suitable linker.
  • the resulting compounds of this invention demonstrate a substantial advantage compared to the use of an uncomplexed active site compound. Furthermore the compounds of this invention show inhibitory activity comparable to hirudin.
  • the compounds of this invention are also stable to enzyme degradation. There is therefore a concrete benefit in using the compounds of this invention as thrombin inhibitors.
  • the compounds of this invention are defined by formula (I) or pharmaceutically acceptable salts thereof: wherein, R is selected from: wherein X 4 is halogen.
  • R 1 is hydrogen, alkyl, alkokyalkyl or aryl.
  • Y is alkyl or aryl.
  • E is guanidyl or amidino.
  • A is a residue of D-pipecolic acid.
  • Z is a divalent straight-chained saturated or unsaturated linker having at least 12 atoms in the chain.
  • P is a peptide of at least 6 amino acid or imino acid residues selected from any fibrinogen recognition exosite portion of a hirudin molecule or analogue thereof.
  • alkyl » represents a saturated or unsaturated; substituted (by a halogen, hydroxyl or C 6-20 aryl) or unsubstituted; straight chain, branched chain, or cyclic hydrocarbon moiety having 1 to 30 carbon atoms and preferably from 1 to 6 carbon atoms this chain or cyclic hydrocarbon moiety may be interrupted by at least one heteroatom such as N, O or S.
  • aryl » represents a carbocyclic moiety which may be substituted by at least one heteroatom (e.g., N, O or S) and containing one benzenoid-type ring preferably containing from 6 to 15 carbon atoms (e.g., phenyl and naphthyl), this carbocyclic moiety may be interrupted by at least one heteroatom such as N, O or S.
  • heteroatom e.g., N, O or S
  • benzenoid-type ring preferably containing from 6 to 15 carbon atoms (e.g., phenyl and naphthyl)
  • aralkyl » represents an aryl group attached to the adjacent atom by an alkyl group (e.g., benzyl), preferably containing from 6 to 30 carbon atoms.
  • alkoxyalkyl represents a substituted or unsubstituted alkyl group containing from 1 to 30 carbon atoms and preferably from 1 to 6 carbon atoms, wherein the alkyl group is covalently bonded to an adjacent element through an oxygen atom (e.g., methoxy and ethoxy).
  • amino acid used herein includes naturally-occurring amino acids as well as non natural analogs as those commonly used by those skilled in the art of chemical synthesis and peptide chemistry.
  • a list of non natural amino acids may be found in "The Peptides", vol. 5, 1983, Academic Press, Chapter 6 by D.C. Roberts and F. Vellaccio. It is to be noted that unless indicated otherwise, the amino acids used in the context of the present invention are those in the L-configuration.
  • a hydrophobic amino acid is usually meant an amino acid that bears an alkyl or aryl group attached to the ⁇ -carbon atom.
  • glycine which has no such group attached to the ⁇ -carbon atom is not a hydrophobic amino acid.
  • the alkyl or aryl group can be substituted, provided that the substituent or substituents present do not detract from the overall hydrophobic character of the amino acid. Water-solubilizing substituents such as OH, COOH and NH 2 are preferably to be avoided.
  • hydrophobic amino acids include natural amino acid residues such as alanine; histidine; isoleucine; leucine; phenylalanine; tryptophane; tyrosine; and unnatural amino acid such as those described in "The Peptides", vol. 5, 1983, Academic Press, Chapter 6 by D.C. Roberts and F. Vellaccio.
  • Subphenylalanine represents the phenylalanine residue bearing substituents on the aromatic ring.
  • Common substituents used by those skilled in the art of amino acid chemistry are halogens (fluoride, bromide, and chloride), electron withdrawing group (NO 2 ) or lower alkyl or aryl substituents in the 2, 3, or 4 position.
  • acidic amino acid is usually meant an amino acid that bears at least one water-solubilizing substituent attached to the ⁇ -carbon atom.
  • Said water-solubilizing substituent is independently selected from the group consisting of alkoxy; carboxylic; hydroxyl; NH 2 ; and carboxyalkyl.
  • glycine which has no such group attached to the ⁇ -carbon atom, is not an acidic amino acid.
  • acidic amino acids includes natural amino acids residues such as serine; threonine; cysteine; tyrosine; asparagine; glutamine; aspartic acid; glutamic acid; lysine; and unnatural amino acids such as those described in "The Peptides", vol. 5, 1983, Academic Press, Chapter 6 by D.C. Roberts and F. Vellaccio.
  • any fibrinogen recognition exosite portion of a hirudin molecule or analogue thereof is meant any portion of a hirudin molecule or analogue thereof which binds to the fibrinogen recognition exosite of thrombin.
  • amino acid residue refers to a dehydrated amino acid, for example the glycine residue is:
  • imino acid residue » refers to a dehydrated cyclic amino acid, for example the proline is :
  • the chiral center shown as * in formula (I) is in the L configuration.
  • Preferred compounds if this invention are defined by formula (I) wherein P is defined by formula (X): G-X 2 -G 1 -Q-X 3 -R 2 wherein,
  • Z may preferably comprise an alkyl chain wherein said alkyl chain may be interrupted by one or more atoms of O, S or N atom, carbonyl or amide group.
  • Z is at least 15 atoms in length and comprises at least one ⁇ -amino acid.
  • Z is at least 15 atoms in length and comprises at least one ⁇ -amino acid.
  • Z is at least 15 atoms in length and comprises a combination of at least one ⁇ -amino acid and at least one ⁇ -amino acid.
  • Z is selected from (12-aminododecanoic acid)-(4-aminobutyric acid)-; (12-aminododecanoic acid)-(6-aminocaproic acid); (8-aminocaprylic acid)-(4-aminobutyric acid)-; (11-aminoundecanoic acid) -glycyl; Glycyl-(12-aminododecanoic acid); (12-aminododecanoic acid)-glycyl; and ⁇ -Alanyl-glycyl-glycyl-5-aminovaleric acid.
  • X 2 is preferrably Phe or Tyr.
  • G and G 1 may independently be: wherein R 3 is wherein R 4 is hydrogen or alkyl; and each R 7 is independently CH 3 or hydrogen.
  • G and G 1 are independently an aspartic acid residue, a glutamic acid residue or a glutamic alkyl ester residue.
  • G and G 1 are independently aspartic or glutamic acid residues.
  • Q is a proline residue or a glutamic acid residue.
  • X 3 is preferrably Ile, Leu, allo-Ile or tert-butyl alanine.
  • R 2 is a oligopeptide having all or a portion of the sequence Pro-Glu-Glu- V - W - X , where V - W is selected from the residues of Tyr-Leu, Tyr-Ala, Tyr-( ⁇ -Cyclohexylalanine), ( ⁇ -cyclohexylalanine)-Leu, Pro-Tyr, Ala-( ⁇ -cyclohexylalanine), Phe-Tyr and, ( ⁇ -cyclohexylalanine)-Ala; and X is D-Glu or Gln.
  • V - W is Tyr-Leu, Tyr-Ala, Tyr-Cha, Cha-Leu, or Cha-Ala.
  • the compounds of this invention are Bzs-Arg-(D-Pip)-Z-P; dansyl-Arg-(D-Pip)-Z-P; dansyl-(D-Arg)-(D-Pip)-Z-P; ⁇ -naphthylsulfonyl-Arg-(D-Pip)-Z-P; ⁇ -naphthylsulfonyl-Arg-(D-Pip)-Z-P; 4-tert-butyl-benzene sulfonyl-Arg-(D-Pip)-Z-P; phenylethyl sulfonyl-Arg-(D-Pip)-Z-P; ⁇ -dihydroanthracenyl- ⁇ -sulfonyl-Arg-(D-Pip)-Z-P; (+)-camphorsulfonyl-Arg-(D-Pip)-Z
  • the ( Z ) portion is preferably (12-aminododecanoic acid)-(4-aminobutyric acid); (12-aminododecanoic acid)-(6-aminocaproic acid); (8-aminocaprylic acid)-(4-aminobutyric acid)-; (12-aminododecanoic acid) -asparagyl-glycyl; (8-aminocaprylic acid) -glycyl; 12-aminododecanoic acid; (11-aminoundecanoic acid)-glycyl; Glycyl-12-aminododecanoic acid); (12-aminododecanoic acid)-glycyl; or ( ⁇ -Alanyl-glycyl-glycyl-5-aminovaleric acid).
  • the ( P ) portion is preferably Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH; Asp-Tyr-Glu-Pro-Ile-Pro-Glu-Glu-Ala-(L- ⁇ -cyclohexylalanine)-(D-Glu)-OH; or Asp-Phe-Glu-Pro-Ile-Pro-Tyr-OH.
  • the biological activity of most of the compounds of this invention were evaluated by two different biological assays.
  • the first assay is an in vitro assay that evaluates the equilibrium dissociation constant (K i ) and the inhibitor concentration required to double the time to fibrinogen clot formation (IC 50 ).
  • the second assay in an in vivo assay that determines both, the dose of the compounds of this invention necessary to double the occlusion time and the dose of the compounds of this invention necessary to achieve patency at 60 min. in a carotid injury-induced thrombosis.
  • the compounds of this invention were exposed to three types of proteases: 1) thrombin, which forms a complex with the inhibitor and may hydrolyse it, 2) plasma proteases encountered by inhibitors during the blood circulation, and 3) kidney proteases, which are heavily involved in the clearance of the peptides.
  • the compounds of this invnetion were very stable to enzyme degradation.
  • the compounds of the present invention show an inhibitory activity comparable to the inhibitory activity of hirudin.
  • table II demonstrate that P448, P531, P532 and P540 have K i values under 0.032 nM.
  • Table III demontrates that P527, P501, P500 and P513 have K i values under 0.027 nM.
  • Table IV shows that P535 and P551 have K i values under 0.00330 nM.
  • Table V shows that BCH-2733 has a K i of 0.8 nM.
  • table VI demonstrate the activity of the compounds of this invention in a carotid induced thrombosis model in the rat mediated by FeCl 3 .
  • Hirulog-8TM is a thrombin inhibitor having a peptide sequence similar to the peptide sequence of hirudin.
  • the results indicate that the compounds of this invention are capable of inhibiting occlusion in the rat carotid artery at doses in the order of ⁇ 0.25 mg/kg i.v.
  • the more preferred compounds of this invention confer full arterial patency at dose as low as 0.5-1 mg/kg i.v whereas Hirulog-8TM which demonstrates patency at 4 mg/kg..
  • the preferred compounds of this invention are:
  • the more preferred compounds of this invention having a K i value smaller then 1 nM are; (P448); (P531); (P532); (P552); (P556); (P540); (P534); (P528); (P527); (P500); (P501);(P498); (P513); (P535); (P551); (P581); (P553); and (BCH-2733).
  • the even more preferred compounds of this invention having a K i value smaller then 0.1 nM are : (P448);(P531);(P532); (P540); (P552); (P527); (P500); (P501); (P513); (P535); (P551); (P553); and (P581).
  • the most preferred compound of this invention is (P553).
  • a compound of the invention may be administered as the raw chemical, it is preferable to present the active ingredient as a pharmaceutical formulation.
  • Pharmaceutically acceptable salts of the compounds of formula (I) include those derived from pharmaceutically acceptable inorganic and organic acids and bases.
  • suitable acids include hydrochloric, hydrobromic, sulphuric, nitric, perchloric, fumaric, maleic, phosphoric, glycollic, lactic, salicylic, succinic, toluene-p-sulphonic, tartaric, acetic, citric, methanesulphonic, formic, benzoic, malonic, naphthalene-2-sulphonic and benzenesulphonic acids.
  • Other acids such as oxalic, while not in themselves pharmaceutically acceptable, may be useful as intermediates in obtaining the compounds of the invention and their pharmaceutically acceptable acid addition salts.
  • the invention thus further provides a pharmaceutical formulation comprising a compound of formula (I) and pharmaceutically acceptable acid addition salt thereof together with one or more pharmaceutically acceptable carriers therefor and, optionally, other therapeutic and/or prophylactic ingredients.
  • the carrier(s) must be "acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
  • a compounds of formula (I) or a pharmaceutically acceptable salt in the manufacture of a medicament for the treatment of vascular disease in a mammal including human.
  • the compounds of the present invention are useful in combinations, formulations and methods for the treatment and prophylaxis of vascular diseases.
  • diseases include myocardial infarction, stroke, pulmonary embolism, deep vein thrombosis, peripheral arterial occlusion, restenosis following arterial injury or invasive cardiological procedures, acute or chronic atherosclerosis, edema and inflammation, cancer and metastasis.
  • the term "combination" as used herein, includes a single dosage form containing at least one compound of this invention and at least one thrombolytic agent, a multiple dosage form, wherein the thrombin inhibitor and the thrombolytic agent are administered separately, but concurrently, or a multiple dosage form wherein the two components are administered separately, but sequentially.
  • the thrombin inhibitor may be given to the patient during the time period ranging from about 5 hours prior to about 5 hours after administration of the thrombolytic agent.
  • the thrombin inhibitor is administered to the patient during the period ranging from 2 hours prior to 2 hours following administration of the thrombolytic agent.
  • the thrombin inhibitor and the thrombolytic agent work in a complementary fashion to dissolve blood clots, resulting in decreased reperfusion times and increased reocclusion times in patients treated with them.
  • the thrombolytic agent dissolves the clot, while the thrombin inhibitor prevents newly exposed, clot-entrapped or clot-bound thrombin from regenerating the clot.
  • the use of the thrombin inhibitor in the formulations of this invention advantageously allows the administration of a thrombolytic reagent in dosages previously considered too low to result in thrombolytic effects if given alone. This avoids some of the undesirable side effects associated with the use of thrombolytic agents, such as bleeding complications.
  • Thrombolytic agents which may be employed in the combinations of the present invention are those known in the art. Such agents include, but are not limited to, tissue plasminogen activator purified from natural sources, recombinant tissue plasminogen activator, streptokinase, urokinase, purokinase, anisolated streptokinase plasminogen activator complex (ASPAC), animal salivary gland plasminogen activators and known, biologically active derivatives of any of the above.
  • tissue plasminogen activator purified from natural sources
  • streptokinase streptokinase
  • urokinase urokinase
  • purokinase purokinase
  • anisolated streptokinase plasminogen activator complex ASPAC
  • animal salivary gland plasminogen activators animal salivary gland plasminogen activators and known, biologically active derivatives of any of the above.
  • compositions and combinations may be employed to administer the formulations and combinations of this invention. These include, but are not limited to, parenteral administration, oral administration and topical application.
  • the formulations and combinations of this invention may be administered to the patient in any pharmaceutically acceptable dosage form, including those which may be administered to a patient intravenously as bolus or by continued infusion, intramuscularly -- including paravertebrally and periarticularly -- subcutaneously, intracutaneously, intra-articularly, intrasynovially, intrathecally, intra-lesionally, periostally or by oral, nasal, or topical routes.
  • Such compositions and combinations are preferably adapted for topical, nasal, oral and parenteral administration, but, most preferably, are formulated for parenteral administration.
  • Parenteral compositions are most preferably administered intravenously either in a bolus form or as a constant infusion.
  • fluid unit dose forms are prepared which contain the compounds of the present invention and a sterile vehicle.
  • the compounds of this invention may be either suspended or dissolved, depending on the nature of the vehicle and the nature of the particular compounds of this invention.
  • Parenteral compositions are normally prepared by dissolving the compounds of this invention in a vehicle, optionally together with other components, and filter sterilizing before filling into a suitable vial or ampule and sealing.
  • adjuvants such as a local anesthetic, preservatives and buffering agents are also dissolved in the vehicle.
  • the composition may then be frozen and lyophilized to enhance stability.
  • Parenteral suspensions are prepared in substantially the same manner, except that the active component is suspended rather than dissolved in the vehicle. Sterilization of the compositions is preferably achieved by exposure to ethylene oxide before suspension in the sterile vehicle.
  • a surfactant or wetting agent is included in the composition to facilitate uniform distribution of its components.
  • Tablets and capsules for oral administration may contain conventional excipients, such as binding agents, fillers, diluents, tableting agents, lubricants, disintegrants, and wetting agents.
  • the tablet may be coated according to methods well known in the art.
  • Suitable fillers which may be employed include cellulose, mannitol, lactose and other similar agents.
  • Suitable disintegrants include, but are not limited to, starch, polyvinylpyrrolidone and starch derivatives, such as sodium starch glycolate.
  • Suitable lubricants include, for example, magnesium stearate.
  • Suitable wetting agents include sodium lauryl sulfate.
  • Oral liquid preparations may be in the form of aqueous or oily suspensions, solutions, emulsions, syrups or elixirs, or may be presented as a dry product for reconstitution with water or another suitable vehicle before use.
  • Such liquid preparations may contain conventional additives.
  • suspending agents such as sorbitol, syrup, methyl cellulose, gelatin, hydroxyethylcellulose, carboxymethylcellulose, aluminum stearate gel or hydrogenated edible fats
  • emulsifying agents which include lecithin, sorbitan monooleate, polyethylene glycols, or acacia
  • non-aqueous vehicles such as almond oil, fractionated coconut oil, and oily esters
  • preservatives such as methyl or propyl p-hydroxybenzoate or sorbic acid.
  • Formulations for topical administration may, for example, be in aqueous jelly, oily suspension or emulsified ointment form.
  • the dosage and dose rate of the compounds of this invention will depend on a variety of factors, such as the weight of the patient, the specific pharmaceutical composition used, the object of the treatment, i.e., therapy or prophylaxis, the nature of the thrombotic disease to be treated, and the judgment of the treating physician.
  • a preferred pharmaceutically effective daily dose of the compounds of this invention is between about 1 ⁇ g/kg body weight of the patient to be treated ("body weight”) and about 5 mg/kg body weight.
  • a pharmaceutically effective daily dose of the thrombolytic is between about 10% and 80% of the conventional dosage range.
  • the "conventional dosage range" of a thrombolytic agent is the daily dosage used when that agent is employed in a monotherapy [physician's Desk Reference 1989, 43rd Edition, Edward R. Barnhart, publisher]. That conventional dosage range will, of course, vary depending on the thrombolytic agent employed.
  • Examples of conventional dosage ranges are as follows: urokinase - 500,000 to 6,250,000 units/patient, streptokinase - 140,000 to 2,500,000 units/patient, tPA - 0.5 to 5.0 mg/kg body weight, ASPAC - 0.1 to 10 units/kg body weight.
  • the therapeutic and prophylactic compositions of the present invention comprise a dosage of between about 10 ⁇ g/kg body weight and about 500 ⁇ g/kg body weight of the compounds of this invention. Most preferred combinations comprise the same amount of the compounds of this invention and between about 10% and about 70% of the conventional dosage range of a thrombolytic agent. It should also be understood that a daily pharmaceutically effective dose of either the compounds of this invention or the thrombolytic agent present in combinations of the invention, may be less than or greater than the specific ranges cited above.
  • a maintenance dose of a combination or composition of this invention is administered, if necessary. Subsequently, the dosage or the frequency of administration, or both, may be reduced, as a function of the symptoms, to a level at which the improved condition is retained. When the symptoms have been alleviated to the desired level, treatment should cease. Patients may, however, require intermittent treatment upon any recurrence of disease symptoms.
  • compounds may be used in compositions and methods for coating the surfaces of invasive devices, resulting in a lower risk of clot formation or platelet activation in patients receiving such devices.
  • Surfaces that may be coated with the compositions of this invention include, for example, prostheses, artificial valves, vascular grafts, stents and catheters. Methods and compositions for coating these devices are known to those of skill in the art. These include chemical crosslinking or physical adsorption of the compounds of this invention-containing compositions to the surfaces of the devices.
  • compounds may be used for the preparation of compositions for ex vivo thrombus imaging in a patient.
  • the compounds of this invention are labelled with a radioisotope.
  • the choice of radioisotope is based upon a number of well-known factors, for example, toxicity, biological half-life and detectability.
  • Preferred radioisotopes include, but are not limited to 125 I, 123 I and 111 I.
  • Techniques for labelling the compounds of this invention are well known in the art. Most preferably, the radioisotope is 123 I and the labelling is achieved using 123 I-Bolton-Hunter Reagent.
  • the labelled thrombininhibitor is administered to a patient and allowed to bind to the thrombin contained in a clot. The clot is then observed by utilizing well-known detecting means, such as a camera capable of detecting radioactivity coupled to a computer imaging system. This technique also yields images of platelet-bound thrombin and meizothrombin.
  • This invention also relates to compositions containing the compounds of this invention for using such compositions in the treatment of tumor metastases.
  • the efficacy of the compounds of this invention for the treatment of tumor metastases is manifested by the inhibition inhibitors to inhibit thrombin-induced endothelial cell activation.
  • This inhibition includes the repression of platelet activation factor (PAF) synthesis by endothelial cells.
  • PAF platelet activation factor
  • These compositions have important applications in the treatment of diseases characterized by thrombin-induced inflammation and edema, which is thought to be mediated be PAF.
  • diseases include, but are not limited to, adult respiratory distress syndrome, septic shock, septicemia and reperfusion damage.
  • Early stages of septic shock include discrete, acute inflammatory and coagulopathic responses.
  • extracorporeal blood includes blood removed in line from a patient, subjected to extracorporeal treatment, and then returned to the patient in such processes as dialysis procedures, blood filtration, or blood bypass during surgery.
  • the term also includes blood products which are stored extracorporeally for eventual administration to a patient and blood collected from a patient to be used for various assays. Such products include whole blood, plasma, or any blood fraction in which inhibition of coagulation is desired.
  • an effective amount of a compounds of this invention of this invention for preventing coagulation in extracorporeal blood is from about 1 ⁇ g/60 ml of extracorporeal blood to about 5 mg/60 ml of extracorporeal blood.
  • the compounds of this invention may also be used to inhibit clot-bound thrombin, which is believed to contribute to clot accretion. This is particularly important because commonly used anti-thrombin agents, such as heparin and low molecular weight heparin, are ineffective against clot-bound thrombin.
  • the compounds of this invention may be employed in compositions and methods for treating neurodegenerative diseases. Thrombin is known to cause neurite retraction, a process suggestive of the rounding in shape changes of brain cells and implicated in neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease.
  • the following examples are set forth. It should be understood that these examples are for illustrative purposes only and are not to be construed as limiting this invention in any manner.
  • Human ⁇ -thrombin (3,000 NIH units/mg), bovine fibrinogen ( ⁇ 70% of protein, 85% of protein clottable), Tos-Gly-Pro-Arg-AMC HCl salt, poly(ethylene glycol) 8000TM, Ada and Tris were purchased from Sigma Inc.
  • AMC dansyl chloride, 1-naphthalenesulfonyl chloride, 2-naphthalenesulfonyl chloride, 4-tert-butylbenzenesulfonyl chloride, Ada, Ava and D,L-Pip were obtained from Aldrich.
  • Boc-Abu, Boc-Bal, Boc-Aca, Boc-Aha, Boc-Cha, Boc-D-Cha, Boc-L-Pip, Boc-D-Pip, and Boc-D-Tic were purchased from BaChem. Acha was obtained from Fluka Inc. Boc-Ada, Boc-D,L-Pip, and Boc-Acha were prepared according to the procedure described by Chaturvedi, D. N., Knittel, J. J., Hruby, V. J., Castrucci, A. M., & Hadley, M. E. (1984) J. Med. Chem. 27, 1406-1410 which is hereby incorporated by reference.
  • Boc-Glu(OBzl)-OH All other amino acid derivatives for peptide synthesis were purchased from Advanced ChemTech except Boc-Glu(OBzl)-OH, which was obtained from Sigma.
  • the side chain protecting groups for Boc-amino acids were benzyl for glutamic acid (Glu) and aspartic acid (Asp), tosyl (Tos) for arginine (Arg) and 2-bromobenzyloxycarbonyl for tyrosine (Tyr).
  • Boc-Gln-OCH 2 -phenylacetylamidomethyl resin (0.714 mmol/g) and p -methyl-benzhydrylamin resin (0.770 mmol/g) were purchased from Applied Biosystems Inc.
  • Boc-D-Glu(OBzl()-OCH2-pheynylacetylamidomethyl resin (0.31 mmol/g) was purchased from Peninsula Laboratories, Inc.
  • the solvents for peptide synthesis were obtained from B&J Chemicals and Applied Biosystems Inc.
  • Citric acid was purchased from Anachemia.
  • HF and TFA were purchased from Matheson and Halocarbon Products Co., respectively.
  • the peptides were prepared according to the method described in Szewczuk, Z., Gibbs, B. F., Yue, S.-Y., Purisima, E., & Konishi, Y. (1992) Biochemistry 31, 9132-9140 which is hereby incorporated by reference. Final products were obtained as lyophilizates with 98% or higher purity estimated by analytical HPLC.
  • the purified peptides were identified by amino acid analysis on a Beckman Model 6300TM high performance analyzer and by molecular mass analysis using a SCIEX API IIITM mass spectrometer. Peptide contents in lyophilizates were determined by the amino acid analysis.
  • Proteolytic stabilities of the compounds of this invention against human ⁇ -thrombin and human plasma proteases were measured as described in Szewczuk et al., 1993, supra, and Szewczuk et al., 1992, supra, respectively.
  • Proteolytic stability of the inhibitors against proteases on kidney membranes was measured as follows: The preparation of kidney membranes was carried out at 0-4°C according to the procedure (method 3) of Maeda, T., Balakrishnan, K., & Mehdi, S. Q. (1983) Biochim. Biophys. Acta 731, 115-120. The kidneys of Sprague-DawleyTM rats were minced finely with surgical scissors.
  • the tissue (1 g) was then added to 3 mL of homogenization buffer (10 mM sodium phosphate buffer, pH 7.4, containing 1 mM MgCl2, 30 mM NaCl, 0.02% NaN3 and 10 ⁇ g/L of DNase) and homogenized using a Polytron* homogenizer (Brinkmann). For sufficient cell disruption,the tissue was subject to five or six bursts for 5 seconds each time at a power setting of 7 separated by 1 to 2 minutes of cooling. About 10 mL of the homogenate was layered over 10 mL of a 41% (w/v) solution of sucroseand centrifuged in a Beckman SW27TM swinging bucket rotor(100000 x g for 30 minutes).
  • the interfacial membranes were collected and washed twice with 10 mM Tris Hcl buffer, pH 7.4.
  • the suspension of the membranes in the same buffer was stored in small aliquots at -80°C until they were used.
  • the protein content of the suspension were determined before the storage by amino acid analysis.
  • An aliquot of kidney membrane (3 mg) and 3 nM of the inhibitor were then incubated in 0.6 mL of 10 mM sodium phosphate buffer, pH 7.4, containing 1 mM MgCl2, 30mM NaCl, 0.02% NaN 3 and 10 ⁇ g/L of DNase, for digestion at 37°C.
  • the chromogenic and fluorogenic substrates Tosyl-Gly-Pro-Arg-pNA and Tos-Gly-Pro-Arg-AMC were purchased from Boehringer Manheim and Sigma, respectively. Fibrinogen and bovine or human ⁇ -thrombins were from Sigma and purity was confirmed by sodium inhibitor dissolved in the same buffer. Initial velocities were recorded at several inhibitor concentrations and kinetic parameters were determined by fitting the data to a general equation describing enzyme inhibition (Segel, 1975). The data were analyzed using the non-linear regression program RNLIN in the IMSL library (IMSL, 1987) on a microVAXTM 3500 computer.
  • the chromogenic and fluorogenic substrates Tosl-Gly-Pro-Arg-pNA and Tos-Gly-Pro-Arg-AMC were purchased from Boehringer Manheim and Sigma, respectively.
  • Fibrinogen and bovine or human ⁇ -thrombins were from Sigma and purity was confirmed by sodium inhibitor dissolved in the same buffer.
  • the fibrin clotting assay was performed in 50 mM Tris HCl buffer (pH 7.52 at 37 °C) containing 0.1 M NaCl and 0.1% poly(ethylene glycol) 8000 with 9.0 x 10-10 M (0.1 NIH unit/mL) and 0.03 % (w/v) of the final concentrations of human thrombin and bovine fibrinogen, respectively, as reported elsewhere (Szewczuk et al., 1992).
  • the clotting time was plotted against the inhibitor concentrations and the IC50 was estimated as the inhibitor concentration required to double the clotting time relative to the control.
  • the inhibition of the amidolytic activity of human thrombin was measured fluorometrically using Tos-Gly-Pro-Arg-AMC as a fluorogenic substrate in 50 mM Tris-HCl buffer (pH 7.52 at 37 °C) containing 0.1 M NaCl and 0.1% poly(ethylene glycol) 8000 at room temperature (Szewczuk et al., 1992).
  • the final concentrations of the inhibitors, the substrate and human thrombin were 0.1-5-fold of Ki, 1-8 x 10 -5 M and 6.0 x 10 -11 M, respectively for the data in Table 1.
  • the corresponding concentrations were 0.5-TM1000-fold of Ki, 1-8 x 10 -6 M and 3.0 x 10 -11 M, respectively, if K, > 10 -10 M, and 10-100-fold of Ki, 5-40 x 10 -6 M and 3.0 10 -11 M, respectively, if Ki ⁇ 10 -10 M.
  • the reaction reached a steady-state within 3 min after mixing thrombin with the substrate and an inhibitor. The steady-state velocity was then measured for a few minutes.
  • the compounds of this invention were also pre-incubated with thrombin for 20 min at room temperature before adding the substrate. The steady-state was achieved within 3 min and measured for a few min.
  • the kinetic data (the steady-state velocity at various concentrations of the substrate and the inhibitors) of the competitive inhibition was analyzed using the methods described by Segel (1975).
  • a non-linear regression program, RNLIN in the IMSL library (IMSL, 1987), LMDER in MINPACK library (More et al., 1980) or MicrosoftTM ExcellTM was used to estimate the kinetic parameters (K m V max and K i ).
  • FeCl3 induced arterial injury model assays were conducted according to Kurz, K.D., Main, R.W., Sandusky, G.E., Thrombosis research 60; 269-280, 1990 and Schumacher, W.A. et al. J. pharmacology and experimental therapeutics 267; 1237-1242, 1993.
  • TTO time to occlusion
  • one blood sample is drawn (1 ml) in a tube of 0.105M buffered citrate solution (from the eye's sinus) and the animal is exsanguinated at the end. All the samples are kept on ice and centrifuged as soon as possible at 2000 Rpm for 10 min., 4°C. The plasma is analyzed in duplicate for activated partial thromboplastin time on a haemostasis analyzer (STAGO ST4TM).

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Claims (27)

  1. Composé de formule (I) ou sels pharmaceutiquement acceptables de ce dernier:
    Figure 00780001
    dans laquelle
    R est choisi dans le groupe constitué de:
    Figure 00780002
    Figure 00780003
    dans lesquelles
    X4 représente un halogène;
    R1 représente l'hydrogène, un alkyle, un alcoxy alkyle ou un aryle;
    Y représente un alkyle ou un aryle;
    E représente le guanidyle ou un amidino;
    A représente un résidu de l'acide D pipécolique;
    Z représente un segment de liaison bivalent à chaíne linéaire, saturé ou insaturé, comptant au moins 12 atomes dans la chaíne; et
    P représente un peptide comptant au moins 6 résidus d'acide aminé ou iminé choisis parmi toute partie d'exosite de reconnaissance du fibrinogène d'une molécule d'hirudine ou d'un analogue de celle-ci;
       dans lequel l'alkyle est un groupe linéaire, ramifié ou cyclique comptant jusqu'à 30 atomes de carbone, facultativement interrompu par un hétéroatome et facultativement substitué par un halogène, OH ou un aryle en C6 à C20; et l'aryle contient au moins un cycle de type benzénoïde comprenant facultativement au moins un hétéroatome.
  2. Composé selon la revendication 1, dans lequel
    R est choisi parmi:
    Figure 00800001
    Figure 00800002
    dans lesquelles
    Y est un alkyle linéaire en C1-C6, un phényléthyle ou un phénylméthyle; et
    E est le guanidyle.
  3. Composé selon la revendication 1, dans lequel le centre chiral * dans la formule (I) est dans le configuration L.
  4. Composé selon la revendication 2, dans lequel le centre chiral * dans la formule (I) est dans la configuration L.
  5. Composé selon la revendication 1, dans lequel P est défini par la formule (X) : G-X2-G1-Q-X3-R2    dans laquelle:
    G et G1 représentent indépendamment des résidus acides d'acide α-aminé;
    X2 représente tout résidu hydrophobe d'acide α-aminé;
    Q est absent ou représente un résidu dérivé d'un acide L-α-aminé ou d'un acide iminé cyclique;
    X3 est absent ou représente tout résidu hydrophobe d'un acide α-aminé; et
    R2 représente un oligopeptide présentant tout ou partie de la séquence Pro Glu-Glu-V-W-X, dans laquelle V et W représentent indépendamment dea résidus hydrophobes d'acide aminé et X représente D-Glu, L-Glu ou Gln.
  6. Composé selon la revendication 1, dans lequel Z représente une chaíne alkyle qui peut être interrompue par un ou plusieurs hétéroatomes choisis parmi O, S et N, un groupe carbonyle ou un groupe amide.
  7. Composé selon la revendication 1, dans lequel Z représente une longueur d'au moins 15 atomes et comprend au moins un acide ω-aminé.
  8. Composé selon la revendication 1, dans lequel Z représente une longueur d'au moins 15 atomes et comprend au moins un acide α-aminé.
  9. Composé selon la revendication 1, dans lequel Z représente une longueur d'au moins 15 atomes et comprend une combinaison d'au moins un acide ω-aminé et d'au moins un acide α-aminé.
  10. Composé selon la revendication 1, dans lequel Z représente [NH- (CHR6)1-11-CO]1 4, [NH- (CH2)1 11-CO]1 4 ou (NHCH2CH=CHCH2CO)3, où R6 est un alkyle ou tout résidu d'acide aminé d'origine naturelle.
  11. Composé selon la revendication 1, dans lequel Z est choisi parmi (acide 12 aminododécanoïque)-(acide 4-aminobutyrique) ; (acide 12 aminododécanoïque)-(acide 6-aminocaproïque); (acide 8-aminocaprylique)-(acide 4-aminobutyrique)-; (acide 11-aminoundécanoïque)-glycyle; glycyl-(acide 12 aminododécanoïque); (acide 12-aminododécanoïque)-glycyle et (β-alanyl glycyl-glycyl)-(acide 5-aminovalérique).
  12. Composé selon la revendication 5, dans lequel:
    G et G1 représentent indépendamment des résidus acides d'acide α-aminé;
    X2 représente Phe ou Tyr;
    Q représente un résidu de proline ou un résidu d'acide glutamique;
    X3 représente Ile, Leu, allo Ile ou tert-butyl-alanine; et
    R2 représente un oligopeptide présentant tout ou partie de la séquence Pro-Glu-Glu-V-W-X, dans laquelle V-W est choisi parmi les résidus de Tyr-Leu, Tyr-Ala, Tyr-(β-cyclohexylalanine), (β cyclohexylalanine)-Leu, Pro-Tyr, Ala-(β-cyclohexylalanine), Phe-Tyr et (β cyclohexylalanine)-Ala; et X représente D-Glu ou Gln.
  13. Composé selon la revendication 12, dans lequel G et G1 représentent indépendamment:
    Figure 00820001
    dans laquelle R3 est choisi parmi:
    Figure 00820002
    Figure 00820003
    où R4 représente l'hydrogène ou un alkyle; et
    chaque R7 représente indépendamment CH3 ou un hydrogène.
  14. Composé selon la revendication 12, dans lequel G et G1 représentent indépendamment un résidu d'acide aspartique, un résidu d'acide glutamique ou un résidu d'alkylester glutamique.
  15. Composé selon la revendication 12, dans lequel G et C1 représentent indépendamment des résidus d'acide aspartique ou glutamique.
  16. Composé selon la revendication 12, dans lequel V W est choisi parmi Tyr-Leu; Tyr-Ala; Tyr-(β-cyclohexylalanine); (β-cyclohexylalanine) Leu; et (β-cyclohexylanaline)-Ala.
  17. Composé selon la revendication 1, qui est le benzylsulfonyl-Arg-(acide D-pipécolique)-Z-P; le dansyl-Arg- (acide D-pipécolique)-Z-P; le dansyl-(D-Arg)-(acide D-pipécolique) -Z-P; l'α-naphtylsulfonyl-Arg-(acide D-pipécolique)-Z-P; le β-naphtylsulfonyl-Arg (acide D-pipécolique) Z-P; le 4-tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-Z-P; le phényléthylsulfonyl Arg (acide D-pipécolique)-Z-P;le β-dihydroanthracényl-β-sulfonyl-Arg-(acide D-pipécolique)-Z-P;le (+)-camphrsulfonyl-Arg-(acide D-pipécolique)-Z-P; le 4-bromo benzènesulfonyl-Arg-(acide D-pipécolique)-Z-P ou le 2,4,6-triisopropylbenzènesulfonyl-Arg (acide D-pipécolique)-Z-P.
  18. Composé selon la revendication 17, dans lequel Z représente l'(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-; l' (acide 12-aminododécanoïque)-(acide 6-aminocaproïque); l'(acide 8-aminocaprylique)-(acide 4-aminobutyrique) -; l' (acide-12 aminododécanoïque) asparagyl glycyle; l'(acide 8-aminocaprylique)-glycyle; l'(acide 12-aminododécanoïque); l'(acide 11-aminoundécanoïque)-glycyle; le glycyl-(acide 12-aminododécanoïque); l'(acide 12-aminododécanoïque)-glycyle ou le (β-alanyl-glycyl-glycyl- (acide 5-aminovalérique)).
  19. Composé selon la revendication 17 ou la revendication 18, dans lequel P représente l'Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH; l'Asp-Tyr-Glu-Pro-Ile-Pro-Glu-Glu-Ala-(L-β-cyclohexylalanine)-(D-Glu)-OH ou l'Asp-Phe-Glu-Pro-Ile-Pro-Tyr-OH.
  20. Composé selon la revendication 17, qui est le dansyl-Arg (acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4 -aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P448);
    le dansyl (D Arg)-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4 aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P492);
    l'α naphtylsulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque) (acide 4-aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P531);
    le β-naphtylsulfonyl Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique) -Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P532);
    le benzylsulfonyl-Arg-(acide D pipécolique)-(acide 12-aminododécanoïque) (acide 4-aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P556);
    le 4-tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu Glu-Tyr-Leu-Gln-OH (P552);
    le (+)-10-camphresulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 6-aminocaproïque)-Asp Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P534);
    le 4-tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 6-aminocaproïque)-Asp Phe Glu Glu Ile Pro Glu-Glu-Tyr-Leu-Gln-OH (P540);
    le dansyl Arg (acide D pipécolique)-(acide 8-aminocaprylique)-glycyl-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr Leu-Gln-OH (P523);
    le dansyl-Arg- (acide D-pipécolique)-(acide 12-aminododécanoïque)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P499);
    le dansyl Arg-(acide D-pipécolique)-(acide 8-aminocaproïque)-(acide 4-aminobutyrique)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P528);
    le dansyl Arg (acide D-pipécolique)-(acide 11-aminoundécanoïque)-glycyl-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P527);
    le dansyl-Arg-(acide D-pipécolique)-glycyl-(acide 12-aminododécanoique)-Asp-Phe-Glu Glu Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P501);
    le dansyl Arg-(acide D-pipécolique)-(acide 12-amino-dodécanoïque), glycyl-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P500);
    le dansyl-Arg-(acide D-pipécolique)-(β-alanyl-glycyl-glycyl (acide 5-aminovalérique) -Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P498);
    le dansyl-Arg (acide D-pipécolique)-(acide 6-aminocaproïque)-(acide 12-aminododécanoïque)-Asp-Phe-Glu-Glu-Ile-Pro-Glu-Glu-Tyr-Leu-Gln-OH (P513);
    le dansyl-Arg- (acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4 aminobutyrique)-Asp-Tyr-Glu-Pro-Ile-Pro-Glu-Glu-Ala-(L-β-cyclohexylalanine)-(D-Glu)-OH (P535);
    le β-naphtylsulfonyl-arginyl-(acide D-pipécolique)-(acide 12-aminododécanoïque)- (acide 4-aminobutyrique)-Asp-Tyr-Glu-Pro-Ile-Pro-Glu-Glu-Ala-(L- β-cyclohexylalanine)-(D-Glu)-OH (P551);
    le 4-tert-butylbenzènesulfonyl-Arg (acide D-pipécolique)-(acide 12 aminododécanoïque)-(acide 4-aminobutyrique) Asp-Tyr-Glu Pro-Ile-Pro-Glu-Glu-Ala- (L-β-cyclohexylalanine)-(D-Glu)-OH (P553);
    l'α-naphtylsulfonyl-arginyl- (acide D-pipécolique) - (acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp-Tyr Glu-Pro-Ile-Pro-Glu-Glu-Ala-(L-β-cyclohexylalanine) (D-Glu) -OH (P581) ;
    le tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp Phe-Glu-Pro-Ile-Pro-Tyr-OH (BCH-2443);
    le tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp-Phe-Glu-Pro-Ile-Pro-Tyr-OH (BCH-2736);
    le tert-butylbenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp-Phe-Glu-Pro-Ile-Pro-Tyr-OH (BCH-2741);
    le 4-bromobenzènesulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp-Phe Clu-Pro-Ile-Pro-Tyr-OH (BCH-2733); et
    le 2,4,6 triisopropylbenzensulfonyl-Arg-(acide D-pipécolique)-(acide 12-aminododécanoïque)-(acide 4-aminobutyrique)-Asp Phe-Glu-Pro-Ile-Pro-Tyr-OH (BCH-2444) .
  21. Composé selon la revendication 20, qui est le (P448); le (P531); le (P532); le (P552); le (P556); le (P540); le (P534); le (P528); le (P527); le (P500); le (P501); le (P498); le (P513); le (P535); le (P551); le (P581); le (P553) ou le (BCH-2733).
  22. Composé selon la revendication 21, qui est le (P448); le (P531); le (P532); le (P540); le (P552); le (P527); le (P500); le (P501); le (P513); le (P535); le (P551); le (P553) ou le (581).
  23. Composé selon la revendication 22, qui est le (P553).
  24. Utilisation d'un composé selon l'une quelconque des revendications précédentes pour la fabrication d'un médicament en vue du traitement de maladies vasculaires chez le mammifère, y compris l'homme.
  25. Composition pharmaceutique comprenant au moins un composé selon l'une quelconque des revendications 1 à 23, en quantité efficace pour traiter ou prévenir des maladies vasculaires, et un porteur pharmaceutiquement acceptable.
  26. Combinaison pharmaceutiquement acceptable pour le traitement ou la prévention des maladies vasculaires chez le mammifère, y compris l'homme, comprenant au moins un composé selon l'une quelconque des revendications 1 à 23; un agent thrombolytique et un porteur pharmaceutiquement acceptable.
  27. Combinaison selon la revendication 26, dans laquelle l'agent thrombolytique est un activateur de plasminogène des tissus.
EP94930133A 1993-10-25 1994-10-25 Inhibiteurs bivalents de thrombine Expired - Lifetime EP0725797B1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB9321951 1993-10-25
GB9321951A GB9321951D0 (fr) 1993-10-25 1993-10-25
GB9412707 1994-06-24
GB9412707A GB9412707D0 (fr) 1993-10-25 1994-06-24
PCT/CA1994/000585 WO1995011921A1 (fr) 1993-10-25 1994-10-25 Inhibiteurs bivalents de thrombine

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EP0725797A1 EP0725797A1 (fr) 1996-08-14
EP0725797B1 true EP0725797B1 (fr) 2001-01-10

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US (1) US6127337A (fr)
EP (1) EP0725797B1 (fr)
AT (1) ATE198603T1 (fr)
AU (1) AU7935494A (fr)
CA (1) CA2175388A1 (fr)
DE (1) DE69426569T2 (fr)
ES (1) ES2153433T3 (fr)
WO (1) WO1995011921A1 (fr)

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EP1023324A1 (fr) * 1997-10-15 2000-08-02 National Research Council Of Canada Inhibiteur de thrombine trivalent
US7829085B2 (en) 1999-07-14 2010-11-09 Life Sciences Research Partners Vzw Methods of treating hemostasis disorders using antibodies binding the C1 domain of factor VIII
SI1278549T1 (sl) 2000-05-02 2009-04-30 Theravance Inc Sestavek, ki vsebuje ciklodekstrin in glikopeptidni antibiotik
EP1706079B1 (fr) 2003-08-14 2013-02-20 ThromboGenics N.V. Anticorps spécifique pour le facteur viii modifiée par glycosylation dans la région variable
US8063018B2 (en) * 2004-06-23 2011-11-22 National Research Council Of Canada Bivalent thrombin binding molecules comprising linkers
AU2005288519A1 (en) * 2004-09-27 2006-04-06 Technion Research & Development Foundation Ltd. Fatty acid modified polylysines as antimicrobial agents
US7915223B2 (en) * 2004-09-27 2011-03-29 Technion Research & Development Foundation Ltd. Antimicrobial agents
WO2006045503A1 (fr) 2004-10-19 2006-05-04 Lonza Ag Procede de synthese de peptides en phase solide
EP2125863A1 (fr) * 2006-12-23 2009-12-02 AplaGen GmbH Procédé de formation de ponts disulfure
WO2008132737A1 (fr) * 2007-04-30 2008-11-06 Technion Research & Development Foundation Ltd. Nouveaux agents antimicrobiens
US20080269065A1 (en) * 2007-04-30 2008-10-30 Syntrix Biosystems, Inc. Conformationally Constrained Analytical Probes
WO2008132738A2 (fr) * 2007-04-30 2008-11-06 Technion Research & Development Foundation Ltd. Agents polymères anticancereux
GB0711779D0 (en) 2007-06-18 2007-07-25 Univ Singapore Thrombin inhibitor
WO2010033249A2 (fr) 2008-09-22 2010-03-25 Massachusetts Institute Of Technology Compositions à base de ligands dimériques et procédés associés
EP2555788B1 (fr) 2010-03-24 2017-10-11 Massachusetts Institute of Technology Dimer du neuregulin pour un erbb/her récepteur pour utilisation dans la réduction de la cardiotoxicité

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US3978045A (en) * 1973-08-13 1976-08-31 Mitsubishi Chemical Industries Ltd. N2 -dansyl-L-arginine derivatives, and the pharmaceutically acceptable acid addition salts thereof
US4173630A (en) * 1974-11-08 1979-11-06 Mitsubishi Chemical Industries Limited N2 Arylsulfonyl-L-argininamides and the pharmaceutically acceptable salts thereof
US5196404B1 (en) * 1989-08-18 1996-09-10 Biogen Inc Inhibitors of thrombin
AU654820B2 (en) * 1990-06-15 1994-11-24 Majesty (Her) In Right Of Canada As Represented By The National Research Council Of Canada Thrombin inhibitors based on the amino acid sequence of hirudin
GB9209032D0 (en) * 1992-04-25 1992-06-10 Ciba Geigy Ag New peptide derivatives

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DE69426569T2 (de) 2001-05-10
DE69426569D1 (de) 2001-02-15
AU7935494A (en) 1995-05-22
CA2175388A1 (fr) 1995-05-04
ES2153433T3 (es) 2001-03-01
EP0725797A1 (fr) 1996-08-14
WO1995011921A1 (fr) 1995-05-04
ATE198603T1 (de) 2001-01-15
US6127337A (en) 2000-10-03

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